Prematurity-Related Ventilatory Control: Role in Respiratory Outcomes (Pre-Vent) - Catalog
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Name
Prematurity-Related Ventilatory Control: Role in Respiratory Outcomes (Pre-Vent)
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Accession Number
HLB03082626a
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Acronym
Pre-Vent
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Related studies
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BSI Study IDs
PRV
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Is public use dataset
False
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Keywords
Obstetric Labor, Premature
Obstetric Labor Complications
Pregnancy Complications
Female Urogenital Diseases and Pregnancy Complications
Urogenital Diseases
Premature Birth -
Ingestion StatusReleased
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Has Study Datasets
True
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Has Specimens
True
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Specimen ID TypeCoded
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Study Website
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The Framingham Heart Study Group requires that the requestor must obtain full or expedited IRB/Ethics Committee review and approval to obtain these data. Waivers or a determination that the research is exempt from ethical regulations do not suffice.
False
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Clinical Trial URLs
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Study typeEpidemiology Study
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Collection TypeOpen BioLINCC Study
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Cohort typePediatric
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Interventions
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Study Open Date (Data)
2026-05-07
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Study Open Date (Specimens)
2026-05-07
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Date materials available
2025-04-03
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Last updated
None
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Study period
March 2018 – June 2021
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Study Contacts
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NHLBI Division
DLD
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ClassificationLung
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HIV study classificationnon-HIV
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COVID study classificationnon-COVID
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Pre-Website # of Specimens Shipped
None
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# of Returned Specimens
None
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Commercial use data restrictionsNo
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Data restrictions based on area of researchYes
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Commercial use specimen restrictionsNo
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Non-genetic use specimen restrictions based on area of useYes
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Genetic use of specimens allowed?Yes
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Genetic use area of research restrictionsYes
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Specific Consent Restrictions
Use of data and/or biospecimens is restricted to research related to breathing problems in infants
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ConditionsInfant, Premature
Prematurity
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Objectives
To develop a predictive model of short-term respiratory outcomes in extremely preterm infants, based on quantitative analysis of neonatal ICU cardiorespiratory monitoring data.
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Background
Preterm birth is a major cause of infant mortality and morbidity worldwide and a leading contributor to disability. Abnormal control of breathing is common in preterm infants and usually manifests as apnea, intermittent hypoxemia, bradycardia, and periodic breathing. Extremely preterm infants may also have impaired gas exchange caused by respiratory distress syndrome and subsequent bronchopulmonary dysplasia. The combination of apnea and lung disease often leads to more prolonged episodes of intermittent hypoxia. Such chronic intermittent hypoxia is associated with worse short-term outcomes (e.g., increased respiratory support, retinopathy of prematurity) and neurodevelopmental impairment that are difficult to predict in the neonatal ICU (NICU). The contribution of abnormal control of breathing to respiratory outcomes has not been determined. The Pre-Vent study was initiated to analyze cardiorespiratory continuous waveform monitoring data to delineate mechanisms of immature ventilatory control in preterm infants and identify predictive markers.
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Participants
Infants less than 29 weeks gestational age with continuously archived cardiorespiratory monitoring data were included. 717 total infants were evaluated.
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Design
Pre-Vent was an observational multicenter prospective cohort study. Clinical data collected included respiratory support, medications, and co-morbidity data. Physiologic data consisted of variables extracted from cardiorespiratory monitoring data and quantified by count of events per day and duration per event. The extracted variables were apnea (≥20 seconds), periodic breathing (wavelet transform using a five-breath template), intermittent hypoxia events with oxygen saturation <80% as measured by pulse oximetry, intermittent hypoxia events with oxygen saturation <90% as measured by pulse oximetry, and bradycardia (<80bpm for 5 seconds or longer).
Infants discharged prior to 40 weeks post-menstrual age or inpatient infants at 40 weeks post-menstrual age had a favorable outcome if they were not on respiratory support or respiratory medications. Infants discharged prior to 40 weeks post-menstrual age or inpatient infants at 40 weeks post-menstrual age had an unfavorable outcome if they were on respiratory medications and/or respiratory support, or deceased.
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Conclusions
The major findings of this study were that mathematical models based on cardiorespiratory bedside monitoring can identify alterations in physiologic measures that are independently associated with unfavorable respiratory outcomes in extremely preterm infants. Both physiologic and clinical variables contributed to good prediction models, with the contribution by physiologic variables increasing with postnatal age.
Weese-Mayer DE, Di Fiore JM, Lake DE, et al. Maturation of cardioventilatory physiological trajectories in extremely preterm infants. Pediatr Res. 2024;95(4):1060-1069. doi:10.1038/s41390-023-02839-0
Ambalavanan N, Weese-Mayer DE, Hibbs AM, et al. Cardiorespiratory Monitoring Data to Predict Respiratory Outcomes in Extremely Preterm Infants. Am J Respir Crit Care Med. 2023;208(1):79-97. doi:10.1164/rccm.202210-1971OC
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Disease classification
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Publications
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Mat typesDNA
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Network
The study population available in BioLINCC study data may be lower than total study enrollment due to Informed Consent restrictions and other factors.
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Subjects
There are 730 participants.
Last Modified: May 29, 2026, 11:42 a.m. -
Age
Preterm infants.
Last Modified: May 29, 2026, 11:42 a.m. -
Sex
Total Subjects
Female
357
Male
373
Last Modified: May 29, 2026, 11:42 a.m. -
Race
Total Subjects
<missing>
691
Unknown/Declined to self-identify
19
Black
8
White
11
American Indian/Native Alaskan/Asian/Other
*S
*Values has been suppressed due to low counts.
Last Modified: May 29, 2026, 11:42 a.m.
Please note that biospecimen availability is subject to review by the NHLBI, BioLINCC, and the NHLBI Biorepository. Certain biospecimens may not be made available for your request. The BioLINCC Users Guide describes the components of the review process.
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Material Types
DNA
Last Modified: May 29, 2026, 11:42 a.m. -
General Freeze/Thaw Status
The vast majority of samples are unthawed.
Last Modified: May 29, 2026, 11:42 a.m. -
Visits (Vials)
Updated 29th May 2026.
DNA
Total
252
252
Last Modified: May 29, 2026, 11:42 a.m. -
Visits (Subjects)
Updated 29th May 2026.
DNA vials are unquantified.
Material
DNA
Total number of subjects
Average vials per subject
136
1.85
Last Modified: May 29, 2026, 11:42 a.m.